Iom Artis Dba, Artis Zeego Multi-axis, Artis Zee Multi-purpose And Ceiling, And Artis Q (2017-11-29)

Siemens Healthineers is recalling certain Axiom Artis and Artis zeego medical imaging systems distributed in Canada due to a potential software issue that could affect image quality and patient safety during procedures. The recall affects multiple Artis model variants including DBA, zeego multi-axis, Zee multi-purpose, Zee ceiling, and Q versions. Healthcare facilities using these systems should contact Siemens Healthineers for further information about the recall.

Reason

Medical devices

Classification

Class I

Category

drug recall

Country

Canada

Agency

HC-DEVICES

Recall date

2017-12-14

Status

Closed

Distribution

Canada-wide

Official recall notice from HC-DEVICES

Recall details on Nibble Recalls: https://trynibble.app/recalls/203c6e11-c3a6-4259-930e-35473c3e8d85